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논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2017.1
- 수록면
- 438 - 442 (5page)
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초록· 키워드
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Choroideremia is a rare X-linked disorder causing progressive chorioretinal atrophy. Affected patients develop night blindness with progressive peripheral vision loss and eventual blindness. Herein, we report two Korean families with choroideremia. Multimodal imaging studies showed that the probands had progressive loss of visual field with characteristic chorioretinal atrophy, while electroretinography demonstrated nearly extinguished cone and rod responses compatible with choroideremia. Sanger sequencing of all coding exons and flanking intronic regions of the CHM gene revealed a novel small deletion at a splice site (c.184_189+3delTACCAGGTA) in one patient and a deletion of the entire exon 9 in the other. This is the first report on a molecular genetic diagnosis of choroideremia in Korean individuals. Molecular diagnosis of choroideremia should be widely adopted for proper diagnosis and the development of new treatment modalities including gene therapy.
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참고문헌 (19)
참고문헌 신청
/ / Exome Aggregation Consortium (ExAC)
Furgoch MJ / 2014 / Molecular genetic diagnostic techniques in choroideremia / Mol Vis 20 : 535 ~ 544
Korea National Research Institute of Health / / Korean Reference Genome Database (KRGDB)
Lee CY / 1981 / Choroideremia / J Korean Ophthalmol Soc 22 : 433 ~ 438
Li S / 2014 / Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosa / Int J Mol Med 34 : 573 ~ 577
Furgoch MJ / 2014 / Molecular genetic diagnostic techniques in choroideremia / Mol Vis 20 : 535 ~ 544
Korea National Research Institute of Health / / Korean Reference Genome Database (KRGDB)
Lee CY / 1981 / Choroideremia / J Korean Ophthalmol Soc 22 : 433 ~ 438
Li S / 2014 / Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosa / Int J Mol Med 34 : 573 ~ 577
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